Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP783046.RAPG5zIX-eNONOpkvAqdDDF20yo6-X7HW0NZ0qxoO_WCE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP783046.RAPG5zIX-eNONOpkvAqdDDF20yo6-X7HW0NZ0qxoO_WCE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP783046.RAPG5zIX-eNONOpkvAqdDDF20yo6-X7HW0NZ0qxoO_WCE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP783046.RAPG5zIX-eNONOpkvAqdDDF20yo6-X7HW0NZ0qxoO_WCE130_provenance.
- NP783046.RAPG5zIX-eNONOpkvAqdDDF20yo6-X7HW0NZ0qxoO_WCE130_assertion description "[Fifty-five adult de novo AML (group A) and 27 elderly AML or AML after myelodysplastic syndrome (AML-MDS) (group B) were tested using probes detecting the following anomalies: -5, -7, +8, deletions of 5q31, 7q31, 12p13/ETV6, 17p13/p53, 20q11.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP783046.RAPG5zIX-eNONOpkvAqdDDF20yo6-X7HW0NZ0qxoO_WCE130_provenance.
- NP783046.RAPG5zIX-eNONOpkvAqdDDF20yo6-X7HW0NZ0qxoO_WCE130_assertion evidence source_evidence_literature NP783046.RAPG5zIX-eNONOpkvAqdDDF20yo6-X7HW0NZ0qxoO_WCE130_provenance.
- NP783046.RAPG5zIX-eNONOpkvAqdDDF20yo6-X7HW0NZ0qxoO_WCE130_assertion SIO_000772 12200689 NP783046.RAPG5zIX-eNONOpkvAqdDDF20yo6-X7HW0NZ0qxoO_WCE130_provenance.
- NP783046.RAPG5zIX-eNONOpkvAqdDDF20yo6-X7HW0NZ0qxoO_WCE130_assertion wasDerivedFrom befree-20140225 NP783046.RAPG5zIX-eNONOpkvAqdDDF20yo6-X7HW0NZ0qxoO_WCE130_provenance.
- NP783046.RAPG5zIX-eNONOpkvAqdDDF20yo6-X7HW0NZ0qxoO_WCE130_assertion wasGeneratedBy ECO_0000203 NP783046.RAPG5zIX-eNONOpkvAqdDDF20yo6-X7HW0NZ0qxoO_WCE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP783046.RAPG5zIX-eNONOpkvAqdDDF20yo6-X7HW0NZ0qxoO_WCE130_provenance.